| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1458546-1458646 | Common:1; Rare:19 | ||||
| chr19:1876131-1876289 | Common:1; Rare:62 | ||||
| chr19:2093079-2093374 | Common:1; Rare:56 | ||||
| chr19:2417114-2417207 | Rare:27 | ||||
| chr19:3125354-3125517 | Common:3; Rare:33 | ||||
| chr19:3131182-3131425 | Common:3; Rare:61 | ||||
| chr19:3152700-3152913 | Common:2; Rare:54 | ||||
| chr19:3153304-3153519 | Common:2; Rare:32 | ||||
| chr19:3507497-3507629 | Common:1; Rare:33 | ||||
| chr19:3977216-3977610 | Common:4; Rare:129; Clinvar (benign):8 | ||||
| chr19:4035798-4035929 | Common:10; Rare:17 | ||||
| chr19:4048707-4048880 | Rare:45 | ||||
| chr19:4053935-4053989 | Rare:21 | ||||
| chr19:4335351-4335704 | Common:3; Rare:76 | ||||
| chr19:4660669-4660956 | Common:7; Rare:76 |